Literature DB >> 11842243

Cytolytic viruses as potential anti-cancer agents.

Christopher J A Ring1.   

Abstract

The resistance of cancers to conventional therapies has inspired the search for novel strategies. One such approach, namely gene therapy, is based upon the introduction of genes such as those encoding suicide proteins, tumour suppressor proteins or cytokines into tumour cells by means of a genetic vector. The efficiency with which viruses transfer their genes from one host cell to another has led to the widespread use of viruses as genetic vectors. For safety reasons, such virus vectors are generally replication-defective but, unfortunately, this has limited the efficacy of treatment by restricting the number of cells to which the therapeutic gene is delivered. For this reason, the use of replication-competent viruses has been proposed, since virus replication would be expected to lead to amplification and spread of the therapeutic genes in vivo. The replication of many viruses results in lysis of the host cells. This inherent cytotoxicity, together with the efficiency with which viruses can spread from one cell to another, has inspired the notion that replication-competent viruses could be exploited for cancer treatment. Some viruses have been shown to replicate more efficiently in transformed cells but it is unlikely that such examples will exhibit a high enough degree of tumour selectivity, and hence safety, for the treatment of patients. Our increasing knowledge of the pathogenesis of virus disease and the ability to manipulate specific regions of viral genomes have allowed the construction of viruses that are attenuated in normal cells but retain their ability to lyse tumour cells. Such manipulations have included modifying the ability of viruses to bind to, or replicate in, particular cell types, while others have involved the construction of replication-competent viruses encoding suicide proteins or cytokines. Naturally occurring or genetically engineered oncolytic viruses based upon adenovirus, herpes simplex virus, Newcastle disease virus, poliovirus, vesicular stomatitis virus, weasles virus and reovirus have been described. The results of animal studies are encouraging and a number of viruses are now being evaluated in clinical trials.

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Year:  2002        PMID: 11842243     DOI: 10.1099/0022-1317-83-3-491

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  25 in total

1.  Vesicular stomatitis virus induces apoptosis in the Wong-Kilbourne derivative of the Chang conjunctival cell line.

Authors:  Eva Gallyas; György Seprényi; Eniko Sonkoly; Yvette Mándi; Lajos Kemény; Klára Megyeri
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2005-11-19       Impact factor: 3.117

2.  p53-expressing conditionally replicative adenovirus CNHK500-p53 against hepatocellular carcinoma in vitro.

Authors:  Hong-Chuan Zhao; Qi Zhang; Yang Yang; Min-Qiang Lu; Hua Li; Chi Xu; Gui-Hua Chen
Journal:  World J Gastroenterol       Date:  2007-02-07       Impact factor: 5.742

3.  Soluble receptor-mediated targeting of mouse hepatitis coronavirus to the human epidermal growth factor receptor.

Authors:  T Würdinger; M H Verheije; K Broen; B J Bosch; B J Haijema; C A M de Haan; V W van Beusechem; W R Gerritsen; P J M Rottier
Journal:  J Virol       Date:  2005-12       Impact factor: 5.103

4.  Rapid adaptation of a recombinant vesicular stomatitis virus to a targeted cell line.

Authors:  Yanhua Gao; Patricia Whitaker-Dowling; Simon C Watkins; Judith A Griffin; Ira Bergman
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

5.  Antitumor activity of an hTERT promoter-regulated tumor-selective oncolytic adenovirus in human hepatocellular carcinoma.

Authors:  Chang-Qing Su; Xing-Hua Wang; Jie Chen; Yong-Jing Liu; Wei-Guo Wang; Lin-Fang Li; Meng-Chao Wu; Qi-Jun Qian
Journal:  World J Gastroenterol       Date:  2006-12-21       Impact factor: 5.742

6.  p53 cooperates with DNA methylation and a suicidal interferon response to maintain epigenetic silencing of repeats and noncoding RNAs.

Authors:  Katerina I Leonova; Leonid Brodsky; Brittany Lipchick; Mahadeb Pal; Liliya Novototskaya; Alex A Chenchik; Ganes C Sen; Elena A Komarova; Andrei V Gudkov
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-10       Impact factor: 11.205

7.  Envelope targeting: hemagglutinin attachment specificity rather than fusion protein cleavage-activation restricts Tupaia paramyxovirus tropism.

Authors:  Christoph Springfeld; Veronika von Messling; Christian A Tidona; Gholamreza Darai; Roberto Cattaneo
Journal:  J Virol       Date:  2005-08       Impact factor: 5.103

Review 8.  Recent trends in targeted anticancer prodrug and conjugate design.

Authors:  Yashveer Singh; Matthew Palombo; Patrick J Sinko
Journal:  Curr Med Chem       Date:  2008       Impact factor: 4.530

9.  Combination of bladder cancer-specific oncolytic adenovirus gene therapy with cisplatin on bladder cancer in vitro.

Authors:  Li Wang; Yunxin Zhang; Jinxia Zhao; Erlong Xiao; Jianzhong Lu; Shengjun Fu; Zhiping Wang
Journal:  Tumour Biol       Date:  2014-08-02

10.  Nuclear accumulation of beta-catenin protein indicates activation of wnt signaling in chemically induced rat nephroblastomas.

Authors:  David Ehrlich; Elisabeth Bruder; Martin A Thome; Carsten N Gutt; Magnus von Knebel Doeberitz; Felix Niggli; Alan O Perantoni; Robert Koesters
Journal:  Pediatr Dev Pathol       Date:  2010 Jan-Feb
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